Catalog Number

00-2500-004-10

Brand Name

Hemovac® Wound Drainage System

Version/Model Number

00-2500-004-10

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

Yes

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

GCY

Product Code Name

Apparatus, Suction, Single Patient Use, Portable, Nonpowered

Public Device Record Key

1c20bf94-4a2f-49c7-bf46-435fe7458795

Public Version Date

February 05, 2021

Public Version Number

2

DI Record Publish Date

September 23, 2020

Package DI Number

00889024378827

Quantity per Package

5

Contains DI Package

00889024372610

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box